MeSH Treeview
Query OMIM entry list
133280
ESD
ESTERASE D
→
High-scoring List
Bacterial Infections and Mycoses
Bacterial Infections
Gram-Positive Bacterial Infections
Actinomycetales Infections
Mycobacterium Infections
Leprosy
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Retinoblastoma
Neoplasms, Glandular and Epithelial
Neoplasms, Neuroepithelial
Retinoblastoma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Retinoblastoma
Neoplasms by Site
Eye Neoplasms
Retinal Neoplasms
Retinoblastoma
Neoplastic Processes
Cell Transformation, Neoplastic
Cell Transformation, Viral
Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Digestive System Diseases
Digestive System Abnormalities
Hirschsprung Disease
Gastrointestinal Diseases
Intestinal Diseases
Colonic Diseases
Megacolon
Hirschsprung Disease
Liver Diseases
Hepatolenticular Degeneration
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Hepatolenticular Degeneration
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Movement Disorders
Hepatolenticular Degeneration
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hepatolenticular Degeneration
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Down Syndrome
Psychomotor Disorders
Eye Diseases
Eye Neoplasms
Retinal Neoplasms
Retinoblastoma
Retinal Diseases
Retinal Neoplasms
Retinoblastoma
Male Urogenital Diseases
Genital Diseases, Male
Penile Diseases
Hypospadias
Urogenital Abnormalities
Hypospadias
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Genital Diseases, Female
Endometriosis
Urogenital Abnormalities
Hypospadias
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Down Syndrome
Chromosome Disorders
Down Syndrome
Digestive System Abnormalities
Hirschsprung Disease
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Urogenital Abnormalities
Hypospadias
Genetic Diseases, Inborn
Chromosome Disorders
Down Syndrome
Heredodegenerative Disorders, Nervous System
Hepatolenticular Degeneration
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Metal Metabolism, Inborn Errors
Hepatolenticular Degeneration
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Papulosquamous
Psoriasis
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Metal Metabolism, Inborn Errors
Hepatolenticular Degeneration
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Chromosome Duplication
Trisomy
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Growth Disorders
Neoplastic Processes
Cell Transformation, Neoplastic
Cell Transformation, Viral
Signs and Symptoms
Body Weight
Body Weight Changes
Weight Gain
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Database Center for Life Science